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  2. Hofmann–Löffler reaction - Wikipedia

    en.wikipedia.org/wiki/Hofmann–Löffler_reaction

    In the reaction, thermal or photochemical decomposition of N-halogenated amine 1 in the presence of a strong acid (concentrated sulfuric acid or concentrated CF 3 CO 2 H) generates a nitrogen radical intermediate. The radical then abstracts an intramolecular hydrogen atom to give a cyclic amine 2 (pyrrolidine or, in some cases, piperidine).

  3. Amine alkylation - Wikipedia

    en.wikipedia.org/wiki/Amine_alkylation

    For example, reaction of 1-bromooctane with ammonia yields almost equal amounts of the primary amine and the secondary amine. [3] Therefore, for laboratory purposes, N-alkylation is often limited to the synthesis of tertiary amines. An exception is the amination of alpha-halo carboxylic acids that do permit synthesis of primary amines with ...

  4. Stieglitz rearrangement - Wikipedia

    en.wikipedia.org/wiki/Stieglitz_rearrangement

    However, there also have been reported examples of base-free Stieglitz rearrangements of N-halogenated amines. An example for that can be found in the total synthesis of (±)-lycopodine by Paul Grieco et al. [6] [29] There, a ring formation takes place by a rearrangement on a secondary haloamine by subjecting it to silver tetrafluoroborate. [6]

  5. N,N-Diisopropylethylamine - Wikipedia

    en.wikipedia.org/wiki/N,N-Diisopropylethylamine

    N,N-Diisopropylethylamine, or Hünig's base, is an organic compound that is a tertiary amine. It is named after the German chemist Siegfried Hünig . It is used in organic chemistry as a non-nucleophilic base. It is commonly abbreviated as DIPEA, DIEA, or i-Pr 2 NEt.

  6. Amine - Wikipedia

    en.wikipedia.org/wiki/Amine

    Amine. In chemistry, amines (/ ə ˈ m iː n, ˈ æ m iː n /, [1] [2] UK also / ˈ eɪ m iː n / [3]) are compounds and functional groups that contain a basic nitrogen atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3 (in which the bond angle between the nitrogen and hydrogen is 107°), wherein one or more hydrogen atoms have been replaced by a substituent such as an ...

  7. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    In chemistry, halogenation is a chemical reaction which introduces one or more halogens into a chemical compound. Halide-containing compounds are pervasive, making this type of transformation important, e.g. in the production of polymers, drugs. [1]

  8. Category:Tertiary amines - Wikipedia

    en.wikipedia.org/wiki/Category:Tertiary_amines

    Pages in category "Tertiary amines" The following 96 pages are in this category, out of 96 total. This list may not reflect recent changes. 0–9. 1P-AL-LAD;

  9. Hydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Hydrohalogenation

    By reaction with tertiary amines, long-chain alkyl bromides such as 1-bromododecane, give quaternary ammonium salts, which are used as phase transfer catalysts. [ 9 ] With Michael acceptors the addition is also anti-Markovnikov because now a nucleophilic X − reacts in a nucleophilic conjugate addition for example in the reaction of HCl with ...